PHAX
Phosphorylated adapter RNA export protein
Also known as: FLJ13193, PHAX_HUMAN, RNUXA
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q9H814
- Gene
- PHAX
- Ensembl
- ENSG00000164902
- Chromosome
- 5
- Canonical length
- 394 aa
- Protein class
- Predicted intracellular proteins, Transporters
- Subcellular location
- Nucleoplasm
OverviewNCBI Gene
Enables mRNA cap binding complex binding activity. Involved in RNA stabilization. Located in nucleoplasm. Part of ribonucleoprotein complex. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
394 residues, UniProt reviewed canonical sequence.
>Q9H814|PHAX
1 MALEVGDMED GQLSDSDSDM TVAPSDRPLQ LPKVLGGDSA MRAFQNTATA CAPVSHYRAV
61 ESVDSSEESF SDSDDDSCLW KRKRQKCFNP PPKPEPFQFG QSSQKPPVAG GKKINNIWGA
121 VLQEQNQDAV ATELGILGME GTIDRSRQSE TYNYLLAKKL RKESQEHTKD LDKELDEYMH
181 GGKKMGSKEE ENGQGHLKRK RPVKDRLGNR PEMNYKGRYE ITAEDSQEKV ADEISFRLQE
241 PKKDLIARVV RIIGNKKAIE LLMETAEVEQ NGGLFIMNGS RRRTPGGVFL NLLKNTPSIS
301 EEQIKDIFYI ENQKEYENKK AARKRRTQVL GKKMKQAIKS LNFQEDDDTS RETFASDTNE
361 ALASLDESQE GHAEAKLEAE EAIEVDHSHD LDIFLocalizationUniProt · AlphaFold · HPA
Whether an antibody against PHAX can act on the native protein depends on physical access: surface and secreted proteins are reachable by circulating antibodies, intracellular proteins usually are not.
- Antibody reachability
- Intracellular
- Secreted
- No
- Transmembrane segments
- 0
- Mean surface accessibility (rSASA)
- 0.54
- Highest tissue expression
- 15 nTPM
Expression across tissuesHPA
Tissue
- cerebral cortex: 15 nTPM
- cerebellum: 14 nTPM
- amygdala: 14 nTPM
- basal ganglia: 13 nTPM
- midbrain: 13 nTPM
- hippocampal formation: 13 nTPM
Single-cell type
- differentiating spermatogonia: 89 nCPM
- early primary spermatocytes: 82 nCPM
- esophageal suprabasal cells: 71 nCPM
- migrating cytotrophoblasts: 68 nCPM
- undifferentiated spermatogonia: 65 nCPM
- cytotrophoblasts: 65 nCPM
Immune cell
- NK-cell: 11 nTPM
- basophil: 8.6 nTPM
- naive CD8 T-cell: 8.2 nTPM
- memory B-cell: 8.1 nTPM
- MAIT T-cell: 8 nTPM
- naive CD4 T-cell: 7.8 nTPM
Brain region
- cerebellum: 26 nTPM
- white matter: 24 nTPM
- cerebral cortex: 23 nTPM
- thalamus: 23 nTPM
- hippocampal formation: 22 nTPM
- amygdala: 21 nTPM
Genetic constraint and essentialitygnomAD · DepMap
Does the body need this protein intact? Low LOEUF or a strong DepMap dependency means loss or blockade of the protein is likely to be felt.
- gnomAD LOEUF (loss-of-function intolerance)
- 0.94
- gnomAD pLI
- 0
- gnomAD missense Z
- 0.48
- DepMap mean gene effect
- -1.13
- DepMap dependency class
- common
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 3% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
- Phosphorylated adapter RNA export protein, RNA-binding domain
- Phosphorylated adapter RNA export protein, RNA-binding domain superfamily
- Phosphorylated adapter RNA export protein
- Phosphorylated adapter RNA export protein, RNA-binding domain
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of PHAX in the human serome: UniProt-annotated complex subunits plus reported interactors. Each links to its own Seroatlas record.
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads PHAX as an antibody target. Whether an autoantibody or antibody against PHAX could matter depends on whether native PHAX is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
PHAX is annotated as predominantly intracellular. Intracellular proteins are common autoantibody markers, becoming visible to the immune system after cell injury or altered processing, but are usually markers of disease rather than direct drivers.
Annotation status
The present source text does not explicitly label PHAX as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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